The Effects of a Walking Program on Balance, Falls and Well Being in Individuals Residing in Long-term Care

The recruitment status of this study is unknown because the information has not been verified recently.
Verified January 2011 by University of Saskatchewan.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
Saskatchewan Health Research Foundation
Information provided by (Responsible Party):
University of Saskatchewan
ClinicalTrials.gov Identifier:
NCT01277809
First received: January 13, 2011
Last updated: August 1, 2012
Last verified: January 2011
  Purpose

The purpose of this study is to assess the effectiveness of a regular walking program (which inevitably involves human interaction) compared to a usual care condition and to a human interaction condition (without the extra walking program) in individuals residing in LTC. Outcomes of interest include: balance, strength, mobility, endurance, walking distance; rate and severity of falls; activities of daily living; mood and behaviour.

It is hypothesized that participants taking part in the walking program will demonstrate maximal benefits compared to the no treatment control group (usual care) and the participants who will only receive social interaction. It is expected that benefits of the walking program will include decreased fall rates, and improved balance, endurance, strength, mood, behaviour, activities of daily living and quality of life indices. Given research findings that the addition of pleasant activities improves resident mood (Teri et al, 1997; 2003), it is expected that participants in the social interaction only group will demonstrate improvements in mood and other indices of quality of life.


Condition Intervention
Accidental Falls
Muscle Weakness
Gait
Depression
Behavior
Behavioral: Interpersonal Interaction
Behavioral: Walking Program

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Community Alliance for Quality of Life in Long Term Care: The Effects of a Walking Program on Balance, Falls and Well Being in Individuals Residing in Long-term Care

Resource links provided by NLM:


Further study details as provided by University of Saskatchewan:

Primary Outcome Measures:
  • Falls [ Time Frame: Eight months ] [ Designated as safety issue: Yes ]
    The incidence and nature of falls will be prospectively collected using a simple daily Fall Diary for the period of the intervention (4 months) and for 4 months following intervention. The Fall Diary will be kept at the residents' bedside and will staff will be asked to record the nature and location of the fall, activity and symptoms at the time of the fall, type of footwear, injuries resulting from the fall. Diaries will be collected every week by study personnel.


Secondary Outcome Measures:
  • Fitness [ Time Frame: Eight months ] [ Designated as safety issue: No ]
    The Senior Fitness Test (SFT) (Rikli & Jones 1999a; 1999b) will assess dynamic upper and lower extremity strength and flexibility, aerobic endurance, and dynamic balance and agility.

  • Balance [ Time Frame: Eight months ] [ Designated as safety issue: Yes ]
    The Berg Balance Scale will be used to objectively assess a person's ability to safely perform several common daily living tasks

  • Grip Strength [ Time Frame: Eight months ] [ Designated as safety issue: No ]
    Grip strength of the dominant and non-dominant hand-held dynamometer will be measured. Strength will be tested 3 times with each hand and the maximum score will be recorded

  • Gait speed [ Time Frame: Eight months ] [ Designated as safety issue: No ]
    Participants will be asked to walk a distance of 6 metres over a portable, computerized walkway (the GAITRite® system (CIR Systems Inc., Clifton, NJ). An additional two metres of walking will be added at the beginning and end of the walkway to accommodate for acceleration and deceleration. Subjects will be asked to walk along the walkway. Gait parameters, including gait speed, will be recorded.

  • Physical Activities of Daily Living [ Time Frame: Eight months ] [ Designated as safety issue: No ]
    OARS Physical Activities of Daily Living (PADL) Sub-Scale (Fillenbaum 1988)will be used as a clinical assessment of functional status. The OARS-PADL will be completed by the research assistant with information provided by subjects' care provider.

  • Depression [ Time Frame: Eight months ] [ Designated as safety issue: No ]
    Mood will be assessed using the Cornell Scale for Depression in Dementia, a well- validated scale designed for the assessment of depression in individuals with dementia and individuals residing in long-term care. The CSDD will be completed by the research assistant with information provided by subjects' care provider.

  • Behavioral problems [ Time Frame: Eight months ] [ Designated as safety issue: No ]
    Behavioral problems will be assessed with the use of the Revised Memory and Behavior Problems Checklist (RMBPC), a 24-item report that measures observable behavioral and memory problems (Appendix). The RMBPC will be completed by the research assistant with information provided by subjects' care provider.

  • Vital signs [ Time Frame: Eight months ] [ Designated as safety issue: Yes ]
    We will measure lying and standing blood pressure as well as heart rate and respiratory rate at baseline and every two months throught the study.


Estimated Enrollment: 179
Study Start Date: December 2010
Estimated Study Completion Date: December 2013
Estimated Primary Completion Date: December 2013 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
No Intervention: Usual Care
Participants will receive care as usual (Usual Care Group; UCG) that is provided by their long-term care unit.
Active Comparator: Interpersonal Interaction
Participants will receive stationary 1:1 interaction time with the same research personnel who conduct the third group walking session at each individual care facility in order to control for the interpersonal interaction likely to be involved in the walking program. This group will receive the equivalent interpersonal interaction time with research personnel as those participating in the walking group. This interaction time will occur with the participant stationary, rather than walking with the researcher.
Behavioral: Interpersonal Interaction
Participants will receive stationary 1:1 interaction time with the same research personnel who conduct the third group walking session at each individual care facility in order to control for the interpersonal interaction likely to be involved in the walking program (Interpersonal Interaction Group; IIG). This group will receive the equivalent interpersonal interaction time with research personnel as those participating in the WPG group. This interaction time will occur with the participant stationary, rather than walking with the researcher.
Experimental: Walking Program
Participants will walk five times per week under the supervision of a licensed physiotherapist.
Behavioral: Walking Program
Participants will walk five times per week, supervised by a licensed physiotherapist. Subjects will in general gradually increase their daily supervised walking time as tolerated to a maximum of 30 minutes once per day. The distance and number of minutes walked each time will be recorded. Interpersonal interaction will occur during the walking sessions, and will be similar in quality and quantity to that during the Interpersonal Interaction Group.

  Eligibility

Ages Eligible for Study:   60 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Adults residing in a long term care facility
  • Able to follow simple instructions
  • Can ambulate with or without a walking aid for at least 10 meters
  • Willing to participate in the study procedures Exclusion Criteria:

Exclusion criteria:

  • Cardiovascular event within past 6 months
  • Severe arthritis
  • Clinical significant vestibular disorder
  • Uncontrolled hypertension
  • Uncontrolled epilepsy
  • Fracture within the past 4 months
  • Admission into an acute care facility in last 4 months
  • Scheduled for surgery or hospitalization in next 6 months
  • Already participating in another regular exercise program (three or more times per week) aimed at improving balance or strength
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01277809

Contacts
Contact: Lilian U Thorpe, MD, PhD (306) 655-7997 lilian.thorpe@saskatoonhealthregion.ca
Contact: Vanina Dal Bello-Haas, Ph.D, P.T. (306) 966-6570 Vanina.Dalbello-Haas@usask.ca

Locations
Canada, Saskatchewan
Saskatoon Health Region Recruiting
Saskatoon, Saskatchewan, Canada, S7K 0M7
Contact: David Gibson    (306)655-8567    David.Gibson@saskatoonhealthregion.ca   
Principal Investigator: Lilian U Thorpe, MD, PhD         
Principal Investigator: Vanina Vanina Dal Bello-Haas, Ph.D, P.T.         
Sub-Investigator: Dennis Alfano, PhD         
Sub-Investigator: Jenny Basran, MD         
Sponsors and Collaborators
University of Saskatchewan
Saskatchewan Health Research Foundation
Investigators
Principal Investigator: Lilian U Thorpe, MD, PhD University of Saskatchewan
Principal Investigator: Vanina Vanina Dal Bello-Haas, Ph. D, P.T. University of Saskatchewan
  More Information

No publications provided by University of Saskatchewan

Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: University of Saskatchewan
ClinicalTrials.gov Identifier: NCT01277809     History of Changes
Other Study ID Numbers: BIO-BEB 10-125
Study First Received: January 13, 2011
Last Updated: August 1, 2012
Health Authority: Canada: Health Canada
Canada: Ethics Review Committee

Keywords provided by University of Saskatchewan:
Long term care
Aging
Accidental Falls
Muscle Weakness
Gait
Physical Fitness
Muscle Strength
Postural Balance
Activities of Daily Living
Body Weight
Blood Pressure
Depression
Behavior
Dementia

Additional relevant MeSH terms:
Depression
Depressive Disorder
Muscle Weakness
Paresis
Behavioral Symptoms
Mental Disorders
Mood Disorders
Muscular Diseases
Musculoskeletal Diseases
Nervous System Diseases
Neurologic Manifestations
Neuromuscular Manifestations
Pathologic Processes
Signs and Symptoms

ClinicalTrials.gov processed this record on October 21, 2014